US4966795A - Multiple layer sheet structures and package - Google Patents

Multiple layer sheet structures and package Download PDF

Info

Publication number
US4966795A
US4966795A US07/192,415 US19241588A US4966795A US 4966795 A US4966795 A US 4966795A US 19241588 A US19241588 A US 19241588A US 4966795 A US4966795 A US 4966795A
Authority
US
United States
Prior art keywords
layer
ethylene
copolymer
component
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US07/192,415
Inventor
Roger P. Genske
Yong J. Kim
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pechiney Plastic Packaging Inc
Original Assignee
American National Can Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US06/802,910 external-priority patent/US4764404A/en
Application filed by American National Can Co filed Critical American National Can Co
Priority to US07/192,415 priority Critical patent/US4966795A/en
Application granted granted Critical
Publication of US4966795A publication Critical patent/US4966795A/en
Assigned to PECHINEY PLASTIC PACKAGINC, INC. reassignment PECHINEY PLASTIC PACKAGINC, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AMERICAN NATIONAL CAN COMPANY
Assigned to PECHINEY PLASTIC PACKAGING, INC. reassignment PECHINEY PLASTIC PACKAGING, INC. DUPLICATE RECORDING, SEE RECORDING AT REEL 012463, FRAME 0131 Assignors: AMERICAN NATIONAL CAN COMPANY
Assigned to PECHINEY EMBALLAGE FLEXIBLE EUROPE reassignment PECHINEY EMBALLAGE FLEXIBLE EUROPE RESUBMISSION OF DOCUMENT ID NO 102198992 Assignors: PECHINEY PLASTIC PACKAGING, INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/16Articles comprising two or more components, e.g. co-extruded layers
    • B29C48/18Articles comprising two or more components, e.g. co-extruded layers the components being layers
    • B29C48/185Articles comprising two or more components, e.g. co-extruded layers the components being layers comprising six or more components, i.e. each component being counted once for each time it is present, e.g. in a layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0807Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
    • C08L23/0815Copolymers of ethene with aliphatic 1-olefins
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1303Paper containing [e.g., paperboard, cardboard, fiberboard, etc.]
    • Y10T428/1307Bag or tubular film [e.g., pouch, flexible food casing, envelope, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1334Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]
    • Y10T428/1338Elemental metal containing
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1355Elemental metal containing [e.g., substrate, foil, film, coating, etc.]
    • Y10T428/1359Three or more layers [continuous layer]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • Y10T428/2817Heat sealable
    • Y10T428/2826Synthetic resin or polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31678Of metal
    • Y10T428/31692Next to addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31678Of metal
    • Y10T428/31692Next to addition polymer from unsaturated monomers
    • Y10T428/31696Including polyene monomers [e.g., butadiene, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31678Of metal
    • Y10T428/31692Next to addition polymer from unsaturated monomers
    • Y10T428/31699Ester, halide or nitrile of addition polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31725Of polyamide
    • Y10T428/31739Nylon type
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31725Of polyamide
    • Y10T428/31739Nylon type
    • Y10T428/31743Next to addition polymer from unsaturated monomer[s]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31725Of polyamide
    • Y10T428/31739Nylon type
    • Y10T428/31743Next to addition polymer from unsaturated monomer[s]
    • Y10T428/31746Polymer of monoethylenically unsaturated hydrocarbon
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/3188Next to cellulosic
    • Y10T428/31895Paper or wood
    • Y10T428/31899Addition polymer of hydrocarbon[s] only
    • Y10T428/31902Monoethylenically unsaturated
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/3188Next to cellulosic
    • Y10T428/31895Paper or wood
    • Y10T428/31906Ester, halide or nitrile of addition polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31913Monoolefin polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31913Monoolefin polymer
    • Y10T428/3192Next to vinyl or vinylidene chloride polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31924Including polyene monomers

Definitions

  • the packaging industry makes and uses many sheet structures in the making of heat sealed packages. Such packages find use in a multiplicity of applications. Of particular interest to the invention herein are those applications where the finished package may be subjected to relatively abusive physical shocks, as by being dropped, bumped, or the like. In cases where the package contains fluid components, the shock may be transferred to all parts of the package by the contained fluid. The transferred shock is effective to cause failure of the package at its weakest point when the severity of shock is sufficiently great.
  • Heat sealed packages tend to fail at or close to a heat seal. Typical failures occur by partial peeling of the facing sealant layers from each other in the seal area. Where the shock is severe enough, the package may have a catastrophic failure wherein the package may be penetrated to the outside.
  • the packages are subjected to heat treatment at elevated temperatures of up to about 250° F. as part of the packaging process.
  • heat treatments are common in certain packaging of medical supplies and shelf stable foods.
  • Some polymers such as polypropylene, which are otherwise excellent for use with high temperature applications, tend to become more brittle after being subjected to such heat treatments. Increasing brittleness leads to less ability to resist shock type abuse. While the use of such materials is desirable for their ability to withstand heat treatment without failure of the package during the heat treatment, the resulting brittleness is an undesirable feature as affects is ability to withstand the shocks of, for example, shipping and handling.
  • Yet another object is to provide heat sealed packages capable of withstanding increased amounts of physical shock type abuse, especially after the closed and sealed package has been subjected to elevated temperatures of up to about 250° F.
  • a first component of the blend is a polypropylene polymer.
  • the second component is an ethylene-based copolymer which consists essentially of ethylene copolymerized with moieties of a second molecule, the composition of said second molecule being selected from the group consisting of propylene and butene-1.
  • said ethylene-based copolymers are sometimes referred to as "EBC").
  • the EBC consists essentially of an ethylene copolymerized with moieties of a second molecule, the copolymer being about 10 to about 95 mole percent ethylene and about 90 to about 5 mole percent of the moieties of the second molecule, the composition of the second molecule being selected from the group consisting of propylene and butene-1.
  • a third component of the blend is an EBC or another elastomeric polymer. (Hereinafter in this application and claims, the aforesaid third component group of materials is sometimes referred to as the "Third Component".)
  • the second component is present in an amount of about 5% to about 35% by weight of the overall composition of the blend.
  • the ethylene-based copolymer is essentially a copolymer of about 85 to about 95 mole percent ethylene and about 15 to about 5 mole percent butene-1.
  • the ethylene-based copolymer is essentially a copolymer of about 60 to about 80 mole percent ethylene and about 40 to about 20 mole percent propylene.
  • the first component be present in an amount of about 40% to about 70% by weight of the overall composition of the blend, and that the third component be present in an amount of about 10% to about 40% by weight.
  • the composition of the third component be selected from the group of elastomers comprising polybutylene, polyisobutylene, ethylene propylene diene monomer terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, polybutene-1, styrene isoprene styrene copolymer, isobutylene isoprene copolymer, or from the EBC group.
  • the first component is present in an amount of about 40% to about 70% by weight
  • the second component is present in an amount of about 5% to about 35% by weight
  • the third component is present in an amount of about 10% to about 40% by weight.
  • the composition of the third component is selected from the group consisting of styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, and polyisobutylene.
  • the invention is also seen to be embodied in single layer films and multiple layer sheet structures made using the novel compositions of the invention.
  • a first layer is made of metal foil, and has two opposing surfaces on opposing sides of the foil layer.
  • a second layer of an abuse resistant polymer is adhered to one of the surfaces on one side of the foil.
  • a third layer is adhered to the sheet structure on the other side of the foil layer.
  • the composition of the third layer is of one of the novel blends of the invention.
  • a first layer is made of a polyamide having two opposing surfaces on opposing sides of the polyamide layer.
  • a second layer of an ethylene vinyl alcohol copolymer has two opposing surfaces. One surface of the second layer is on one surface on one side of the first layer.
  • a third layer of a polyamide is on the other surface of the second layer opposite the first layer.
  • a fourth layer is adhered to the sheet structure on the other side of the first layer.
  • the composition of the fourth layer is one of the novel blends of the invention.
  • a first layer is made of a barrier material having two opposing surfaces, on opposing sides of the first layer, the composition of the first layer being a vinylidene chloride copolymer.
  • a second layer is made of an abuse resistant polymer adhered to one surface on one side of the first layer.
  • a third layer is adhered, in the sheet structure, on the other side of the first layer.
  • the composition of the third layer is one of the novel blends of the invention.
  • Packages which may or may not be heat sealed, may also be made of the films and sheet structures of the invention.
  • FIG. 1 is a cross-section of a portion of a 2-layer film of the invention.
  • FIG. 2 is a cross-section of a portion of a 3-layer sheet structure of the invention, and using a layer of a metal foil as a barrier layer.
  • FIG. 3 is a cross-section of a portion of a 4-layer film of the invention.
  • FIG. 4 is a cross-section of a portion of another 3-layer film of the invention, and using a polymeric barrier material as the internal layer.
  • FIG. 5 is a pictorial view of a typical pouch made in the invention.
  • the invention encompasses a plurality of forms and embodiments. In its most generic form, it is a composition of matter formed by the intimate blending together of the blend components. It may also be represented by a variety of articles which can be formed such as by molding or extruding the blend composition. A preferred form of article so fabricated is a single layer packaging film which may be formed by conventional extrusion process. Such films are typically thin and flexible, being of the order of about 1 mil to about 8 mils thick. Thicker sections and shapes may also be formed, as for other uses.
  • layer 12 is a layer of a novel blend composition embodied in the invention.
  • Layer 14 is a layer of an abuse resistant polymer, such as polypropylene.
  • FIG. 1 illustrates a simpler form of packages of the invention. It is advantageous in its simplicity, and may find use in applications where high levels of protection from gaseous infusion are not so important.
  • layer 16 is a layer of metal foil, which provides an excellent barrier to gaseous infusion.
  • layer 14 is a layer of an abuse resistant polymer as in FIG. 1.
  • Layer 12 is a layer of a blend composition of the invention.
  • the structure of FIG. 2 is representative of a sheet structure useful in making retortable pouches. Such structures may also be used for applications where the package is not subjected to retort conditions. In those cases, the specific materials selected for each layer need not be evaluated in terms of their ability to withstand the retorting process. Typical problems encountered in retort processing are excessive softening during the processing, or embrittlement resulting from the processing.
  • the foil layer 16 of such a retortable package is commonly 28 gauge to 100 gauge, with the thinner gauges being preferred for economic reasons.
  • the abuse resistant layer 14 may be any of the conventionally known abuse resistant polymers. These include, for example, nylon, oriented nylon, oriented polypropylene, and oriented polyester.
  • layer 14 is typically about 50 gauge, with a range of about 25 gauge to about 100 gauge. It is conventionally known to achieve adhesion between the foil layer 16 and abuse resistant layer 14 by means of adhesives such as polyester urethane curing type adhesives. These adhesives are acceptable for such use herein.
  • the blend layer 12 may be any of the blend compositions of the invention.
  • the FIG. 2 structure is designed such that layer 12 may be used as a heat seal layer.
  • a minimum thickness for achieving strong heat seals is about 1 mil; so that is a preferred minimum thickness.
  • Thicker heat seal layers may advantageously provide more efficient use in heat seal material, up to about 4 mils; and that is a generally preferred maximum thickness.
  • layer 12 may be much thicker, for example about 8 or more mils, and same is encompassed by the scope of the invention, no material benefit is usually seen to be derived from the use of the additional material; so the greater thicknesses are not generally preferred.
  • Layer 12 may be adhered to layer 16 by a conventional polyester urethane curing type adhesive. Alternately, adhesion may be achieved by other methods such as by extrusion lamination, coextrusion lamination, or extrusion coating followed by heat and pressure at a hot nip. In some instances, it may be desirable to use a primer on the surface of foil layer 16 before adhering layers 12 and 16 to each other.
  • layer 12 is a blend composition of the invention as in FIGS. 1 and 2.
  • Layer 18 is a polyamide.
  • Layer 20 is an ethylene vinyl alcohol copolymer.
  • Layer 22 is a polyamide.
  • FIG. 3 represents generically a family of sheet structures which provide effective barrier to transmission of oxygen through the sheet structure while affording transparency of the packaging material for visibility of the packaged contents. These packages do have a variety of uses; and the selection of specific polymers and combinations of polymers depends on the particular use contemplated. A typical use is, as for the structure of FIG. 2, that of retort packaging.
  • an adhesive such as an adhesive polymer
  • adhesive polymer Typical of these adhesive polymers are those based on polypropylene and having carboxyl modifications thereto, such as maleic acid or maleic anhydride.
  • the structure may, of course, be made by other processes but they generally will be more expensive, and thus those processes are less preferred.
  • adhesive lamination wherein the layers may be joined by using, for example, polyester urethane curing type adhesive.
  • polyamide as used in describing the compositions of layers 18 and 22 is intended to include copolymers and alloys of polyamide as a major component. Likewise, additives which are normally used with polyamide are acceptable herein and are thus included in the compositions of layers 18 and 22. While the compositions of layers 18 and 22 are usually the same, to facilitate coextrusion of the sheet material, they may be different and the process adapted accordingly.
  • ethylene vinyl alcohol copolymer as used in describing the composition of layer 20, is intended to include blends of ethylene vinyl alcohol with other polymers. Likewise, additives which are normally used with ethylene vinyl alcohol copolymer are acceptable herein and are thus included in the composition of layer 20.
  • elastomeric includes polymers, copolymers, rubbers, and the like which at room temperature can be stretched substantially under low stress and, upon immediate release of the stress, have the tendency to return generally to approximately the original shape.
  • the blend layer 12 may be any of the blend compositions of the invention.
  • the FIG. 3 structure, as in FIGS. 1 and 2, is designed such that layer 12 may be used as a heat seal layer.
  • a minimum thickness for achieving strong heat seals is likewise about 1 mil in this structure; so that is a preferred minimum thickness.
  • Thicker heat seal layers may advantageously provide more efficient use of the heat seal material, up to about 4 mils; so that is a generally preferred maximum thickness.
  • Layer 12 may also be thicker, as described for the corresponding layer 12 in FIG. 2.
  • Layer 12 may also be less than 1 mil thick, as, for example, in all the illustrated embodiments, where heat seals are not used or seal strength is not critical.
  • layer 14 is an abuse resistant layer as in FIG. 2.
  • Layer 12 is of a blend composition of the invention as in FIGS. 1-3.
  • Layer 24 is an oxygen barrier layer such as vinylidene chloride copolymer. Preferred copolymers are vinylidene chloride-vinyl chloride copolymer and vinylidene chloride-methylacrylate copolymer.
  • layer 24 is usually of a thickness of 0.3 to 2.0 mil, depending primarily on the rate of oxygen transmission which is desired for any given end use. While adhesion may be achieved by other means, suitable adhesives, such as the polyester urethane curing adhesives, are usually economically used between the respective layers 12, 24, and 14 to achieve good adhesion between the layers.
  • layers 12, 24, and 14 are usually formed separately from each other and then combined into the multiple layer structure shown, by conventional techniques for combining polymer films. In a typical process, the layers are joined by conventional adhesive lamination techniques.
  • the blend composition of polypropylene and the second and third components has useful advantage in a variety of multiple layer structures.
  • a layer of the blend composition may advantageously be used in combination with any other layer which may be adhered to it.
  • the multiple layer embodiment of the invention may be generically defined as a multiple layer sheet material wherein the composition of at least one layer is comprised of a blend of polypropylene and the second and third components; and wherein the composition of the other layer or layers need not necessarily be restricted except for purposes of obtaining interlayer adhesion acceptable to the intended use.
  • non-polymeric materials such as paper and metal foil, and the like, may be used, as well as polymeric materials.
  • the multiple layer sheet structures of the invention are advantageously formed into packages using heat seals, as illustrated in FIG. 5.
  • portions of the sheet material are brought into face-to-face relationship, with the layers 12 on each portion facing the opposing sheet portion.
  • Heat seals 28 are then formed between the sheet portions about a common periphery to form a container 30 that generally defines an enclosed area.
  • one side of the thus formed package is left open, as shown, for insertion of the product.
  • the filled package is closed and sealed by a heat seal along the open side.
  • the sheet may be formed into a tube by forming a longitudinal seal along overlapping edges; and a transverse seal is also formed across the width of the tube; all as described, for example, in U.S. Pat. No. 4,521,437, herein incorporated by reference. This process is particularly suitable for use in vertical form, fill and seal machines.
  • the ethylene-based copolymer of the second component is essentially a copolymer of two moieties, both moieties being present in the main chain of the polymer.
  • the overall mole ratio is about 10 to about 95 mole percent ethylene, and conversely about 90 to about 5 mole percent of the second moiety.
  • the ethylene is preferably copolymerized with propylene or butene-1. In the case of propylene, the mole ratio is most preferably within the range of about 20% to about 40% propylene and about 80% to about 60% ethylene.
  • TAFMER P One such material is sold by Mitsui Petrochemical Industries, Ltd. as TAFMER P.
  • the mole ratio is most preferably within the range of about 85% to about 95% ethylene, and about 15% to about 5% butene-1.
  • TAFMER A is sold by Mitsui Petrochemical Industries, Ltd. as TAFMER A.
  • TAFMER P is elastomeric.
  • Tafmer A provides some properties representative of elastomers, as seen in the following EXAMPLES herein.
  • the third component may be any of the known and readily available elastomeric polymers, or an EBC, indeed even blends thereof.
  • readily available elastomeric polymers are polybutylene, polyisobutylene, ethylene propylene diene monomr terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, polybutene-1, and isobutylene isoprene copolymer.
  • the third component is not, however, the same as the second component, as such would effectively make a two-component blend, rather than a three component blend as defined in the invention.
  • the polypropylene which is used as the first component of the blend provides strength to the sheet structure as well as the capability to withstand high temperature without excessive softening.
  • the inclusion of the second and third components in the blend composition provides resilience to the blend composition.
  • any of the polypropylenes may be used in the first component of the blend.
  • Polypropylenes which are copolymers having about 2 to about 8 mole percent ethylene are preferred, as the copolymer provides some minimum level of additional resilience to the polypropylene, as compared to a homopolymer.
  • the term "polypropylene" as used herein is intended to include homopolymers and copolymers except where specified otherwise. Whether the polypropylene is a homopolymer or copolymer, its resilience as demonstrated herein, whether having been retort processed, or not retort processed, is enhanced substantially by the incorporation of the second and third components. Without the incorporation of the second and third components, the polypropylene is at least somewhat rigid, whether homopolymer or copolymer.
  • a blend of 60% by weight of the polypropylene and 40% polyisobutylene is superior to the same polypropylene when tested in unblended composition, as measured in free fall drop tests of the packages. But these packages with polyisobutylene will fail, at a 9 foot drop with the failure being by rupture through the package wall adjacent a heat seal.
  • packages were made using single-layer film whose composition was 60% by weight of the same polypropylene copolymer, 20% TAFMER A and 20% polyisobutylene, for the same total weight of 40% by weight elastomer as in the above packages using two-component blends.
  • the resulting packages passed the 9 foot drop tests, which passage was not found for either of the 2-component blends.
  • polypropylene homopolymer While polypropylene homopolymer is fully satisfactory for many uses, the polypropylene copolymer is preferred, as it evidences the optimum properties of improved resistance to shock abuse in combination with the capability to withstand elevated processing temperatures. Optimum performance is generally seen, then, in blends of polypropylene copolymer with the second and third components.
  • polypropylene may be present in an amount of about 10% to about 95% by weight, a generally preferred range is about 40% to about 70%.
  • a lower level of about 40% is generally preferred in order to maintain at least a minimal degree of the high heat temperature tolerance of the composition, and a significant moisture vapor barrier, which are provided by polypropylene.
  • An upper level of 70% is generally desired.
  • the incorporation of virtually any amount of the second component into the blend composition will provide some benefit, generally, improvement are first evident at a level of about 2% by weight. And while up to about 70% of the second component may be used, the most desired balance of properties is achieved when the second component is present in an amount of about 5% to about 35%.
  • the incorporation of virtually any amount of the third component into the blend composition will provide some benefit, generally, inprovements are first evident at a level of about 2% by weight. And while up to about 60% of the third component may be used, the most desired balance of properties is achieved when the third component is present in an amount of about 10% to about 40%.
  • compositions of the invention are that where each of the components is within its preferred range of compositions; namely about 40% to about 70%. polypropylene, about 5% to about 35% of the second component, and about 10% to about 40% of the third component.
  • the invention provides novel material blend compositions.
  • the invention further provides single layer films and multiple layer films and sheet structures for use in making packages.
  • the invention provides heat sealed packages capable of withstanding substantial amounts of physical shock type abuse, which capability is especially noticeable after the closed and sealed packages have been subjected to elevated temperatures of up to about 250° F.

Abstract

Sheet structures wherein the composition of one layer comprises a first component of a polypropylene, a second component of an ethylene-based copolymer, and a third component which provides some properties representative of elastomeric polymers. The invention further contemplates packages made from the sheet structures incorporating the recited compositions.

Description

This is a continuation of application Ser. No. 802,910, filed Nov. 29, 1985, now U.S. Pat. No. 4,764,404.
BACKGROUND OF THE INVENTION
The packaging industry makes and uses many sheet structures in the making of heat sealed packages. Such packages find use in a multiplicity of applications. Of particular interest to the invention herein are those applications where the finished package may be subjected to relatively abusive physical shocks, as by being dropped, bumped, or the like. In cases where the package contains fluid components, the shock may be transferred to all parts of the package by the contained fluid. The transferred shock is effective to cause failure of the package at its weakest point when the severity of shock is sufficiently great.
Heat sealed packages tend to fail at or close to a heat seal. Typical failures occur by partial peeling of the facing sealant layers from each other in the seal area. Where the shock is severe enough, the package may have a catastrophic failure wherein the package may be penetrated to the outside.
Such failure of the package, whether by partial peeling or by catastrophic failure, compromises the containment and protective functions of the package, and is thus not acceptable. It is desirable to find material compositions which may be used in packaging sheet structures which compositions enhance the capability of the sheet structure, and particularly the sealant layer, to withstand increased amounts of shock-type abuse.
In certain packaging applications, the packages are subjected to heat treatment at elevated temperatures of up to about 250° F. as part of the packaging process. Such heat treatments are common in certain packaging of medical supplies and shelf stable foods.
Some polymers, such as polypropylene, which are otherwise excellent for use with high temperature applications, tend to become more brittle after being subjected to such heat treatments. Increasing brittleness leads to less ability to resist shock type abuse. While the use of such materials is desirable for their ability to withstand heat treatment without failure of the package during the heat treatment, the resulting brittleness is an undesirable feature as affects is ability to withstand the shocks of, for example, shipping and handling.
It is an objective of this invention to provide novel material blend compositions.
It is further object of this invention to provide single layer films and multiple layer films and sheet structures, incorporating therein the novel compositions, for use in making packages, and particularly heat sealed packages.
Yet another object is to provide heat sealed packages capable of withstanding increased amounts of physical shock type abuse, especially after the closed and sealed package has been subjected to elevated temperatures of up to about 250° F.
SUMMARY OF THE DISCLOSURE
These and other objectives are obtained in the novel compositions, films, sheet structures, and packages of the invention. In the novel blend compositions, a first component of the blend is a polypropylene polymer. The second component is an ethylene-based copolymer which consists essentially of ethylene copolymerized with moieties of a second molecule, the composition of said second molecule being selected from the group consisting of propylene and butene-1. (Hereinafter, said ethylene-based copolymers are sometimes referred to as "EBC"). Preferably the EBC consists essentially of an ethylene copolymerized with moieties of a second molecule, the copolymer being about 10 to about 95 mole percent ethylene and about 90 to about 5 mole percent of the moieties of the second molecule, the composition of the second molecule being selected from the group consisting of propylene and butene-1. A third component of the blend is an EBC or another elastomeric polymer. (Hereinafter in this application and claims, the aforesaid third component group of materials is sometimes referred to as the "Third Component".)
Preferably, the second component is present in an amount of about 5% to about 35% by weight of the overall composition of the blend.
In one preferred embodiment, the ethylene-based copolymer is essentially a copolymer of about 85 to about 95 mole percent ethylene and about 15 to about 5 mole percent butene-1.
In another preferred embodiment, the ethylene-based copolymer is essentially a copolymer of about 60 to about 80 mole percent ethylene and about 40 to about 20 mole percent propylene.
Turning now to the blend as a whole, it is preferred that the first component be present in an amount of about 40% to about 70% by weight of the overall composition of the blend, and that the third component be present in an amount of about 10% to about 40% by weight. It is preferred that the composition of the third component be selected from the group of elastomers comprising polybutylene, polyisobutylene, ethylene propylene diene monomer terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, polybutene-1, styrene isoprene styrene copolymer, isobutylene isoprene copolymer, or from the EBC group.
In one family of preferred overall compositions, the first component is present in an amount of about 40% to about 70% by weight, the second component is present in an amount of about 5% to about 35% by weight, and the third component is present in an amount of about 10% to about 40% by weight. In that family of preferred overall compositions, the composition of the third component is selected from the group consisting of styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, and polyisobutylene.
The invention is also seen to be embodied in single layer films and multiple layer sheet structures made using the novel compositions of the invention.
In one multiple layer sheet structure of the invention, a first layer is made of metal foil, and has two opposing surfaces on opposing sides of the foil layer. A second layer of an abuse resistant polymer is adhered to one of the surfaces on one side of the foil. A third layer is adhered to the sheet structure on the other side of the foil layer. The composition of the third layer is of one of the novel blends of the invention.
In another multiple layer sheet structure of the invention, a first layer is made of a polyamide having two opposing surfaces on opposing sides of the polyamide layer. A second layer of an ethylene vinyl alcohol copolymer has two opposing surfaces. One surface of the second layer is on one surface on one side of the first layer. A third layer of a polyamide is on the other surface of the second layer opposite the first layer. A fourth layer is adhered to the sheet structure on the other side of the first layer. The composition of the fourth layer is one of the novel blends of the invention.
In yet another multiple layer sheet structure of the invention, a first layer is made of a barrier material having two opposing surfaces, on opposing sides of the first layer, the composition of the first layer being a vinylidene chloride copolymer. A second layer is made of an abuse resistant polymer adhered to one surface on one side of the first layer. A third layer is adhered, in the sheet structure, on the other side of the first layer. The composition of the third layer is one of the novel blends of the invention.
Packages, which may or may not be heat sealed, may also be made of the films and sheet structures of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a cross-section of a portion of a 2-layer film of the invention.
FIG. 2 is a cross-section of a portion of a 3-layer sheet structure of the invention, and using a layer of a metal foil as a barrier layer.
FIG. 3 is a cross-section of a portion of a 4-layer film of the invention.
FIG. 4 is a cross-section of a portion of another 3-layer film of the invention, and using a polymeric barrier material as the internal layer.
FIG. 5 is a pictorial view of a typical pouch made in the invention.
DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS
The invention encompasses a plurality of forms and embodiments. In its most generic form, it is a composition of matter formed by the intimate blending together of the blend components. It may also be represented by a variety of articles which can be formed such as by molding or extruding the blend composition. A preferred form of article so fabricated is a single layer packaging film which may be formed by conventional extrusion process. Such films are typically thin and flexible, being of the order of about 1 mil to about 8 mils thick. Thicker sections and shapes may also be formed, as for other uses.
Other preferred embodiments of the invention are those where the blend composition is used to form one layer of a multiple layer sheet structure. Representative of these sheet structures are those illustrated in FIGS. 1-4. Other sheet structures are possible, and contemplated.
Turning now to FIG. 1, layer 12 is a layer of a novel blend composition embodied in the invention. Layer 14 is a layer of an abuse resistant polymer, such as polypropylene.
The structure of FIG. 1 illustrates a simpler form of packages of the invention. It is advantageous in its simplicity, and may find use in applications where high levels of protection from gaseous infusion are not so important.
Where protection from gaseous infusion is more important, a layer of a barrier material is used. In the structure of FIG. 2, layer 16 is a layer of metal foil, which provides an excellent barrier to gaseous infusion. Layer 14 is a layer of an abuse resistant polymer as in FIG. 1. Layer 12 is a layer of a blend composition of the invention.
The structure of FIG. 2 is representative of a sheet structure useful in making retortable pouches. Such structures may also be used for applications where the package is not subjected to retort conditions. In those cases, the specific materials selected for each layer need not be evaluated in terms of their ability to withstand the retorting process. Typical problems encountered in retort processing are excessive softening during the processing, or embrittlement resulting from the processing. The foil layer 16 of such a retortable package is commonly 28 gauge to 100 gauge, with the thinner gauges being preferred for economic reasons. The abuse resistant layer 14 may be any of the conventionally known abuse resistant polymers. These include, for example, nylon, oriented nylon, oriented polypropylene, and oriented polyester. For use in retort packaging, layer 14 is typically about 50 gauge, with a range of about 25 gauge to about 100 gauge. It is conventionally known to achieve adhesion between the foil layer 16 and abuse resistant layer 14 by means of adhesives such as polyester urethane curing type adhesives. These adhesives are acceptable for such use herein.
The blend layer 12 may be any of the blend compositions of the invention. The FIG. 2 structure is designed such that layer 12 may be used as a heat seal layer. A minimum thickness for achieving strong heat seals is about 1 mil; so that is a preferred minimum thickness. Thicker heat seal layers may advantageously provide more efficient use in heat seal material, up to about 4 mils; and that is a generally preferred maximum thickness. While layer 12 may be much thicker, for example about 8 or more mils, and same is encompassed by the scope of the invention, no material benefit is usually seen to be derived from the use of the additional material; so the greater thicknesses are not generally preferred.
Layer 12 may be adhered to layer 16 by a conventional polyester urethane curing type adhesive. Alternately, adhesion may be achieved by other methods such as by extrusion lamination, coextrusion lamination, or extrusion coating followed by heat and pressure at a hot nip. In some instances, it may be desirable to use a primer on the surface of foil layer 16 before adhering layers 12 and 16 to each other.
Turning next to FIG. 3, layer 12 is a blend composition of the invention as in FIGS. 1 and 2. Layer 18 is a polyamide. Layer 20 is an ethylene vinyl alcohol copolymer. Layer 22 is a polyamide.
The structure of FIG. 3 represents generically a family of sheet structures which provide effective barrier to transmission of oxygen through the sheet structure while affording transparency of the packaging material for visibility of the packaged contents. These packages do have a variety of uses; and the selection of specific polymers and combinations of polymers depends on the particular use contemplated. A typical use is, as for the structure of FIG. 2, that of retort packaging.
It is known to coextrude a multiple layer film structure wherein a layer of ethylene vinyl alcohol copolymer is between two layers of polyamide. Such a structure is seen in the substructures of layers 18, 20 and 22. It has been found further acceptable to including layer 12 as part of the coextrusion. Thus, the structure of FIG. 3 may be advantageously and economically produced in a single processing step by coextruding all four layers simultaneously and combining them in the coextrusion process to form the multiple layer sheet structure.
For enhanced adhesion between layers 12 and 18, it is sometimes desirable to include an adhesive, such as an adhesive polymer, between layers 12 and 18. Such materials are conventionally known and may be selected based on the specific compositions of layers 12 and 18 and the process to be used. Typical of these adhesive polymers are those based on polypropylene and having carboxyl modifications thereto, such as maleic acid or maleic anhydride.
The structure may, of course, be made by other processes but they generally will be more expensive, and thus those processes are less preferred. illustrative of these is adhesive lamination wherein the layers may be joined by using, for example, polyester urethane curing type adhesive.
The term polyamide, as used in describing the compositions of layers 18 and 22 is intended to include copolymers and alloys of polyamide as a major component. Likewise, additives which are normally used with polyamide are acceptable herein and are thus included in the compositions of layers 18 and 22. While the compositions of layers 18 and 22 are usually the same, to facilitate coextrusion of the sheet material, they may be different and the process adapted accordingly.
The term ethylene vinyl alcohol copolymer as used in describing the composition of layer 20, is intended to include blends of ethylene vinyl alcohol with other polymers. Likewise, additives which are normally used with ethylene vinyl alcohol copolymer are acceptable herein and are thus included in the composition of layer 20.
The term "elastomeric" includes polymers, copolymers, rubbers, and the like which at room temperature can be stretched substantially under low stress and, upon immediate release of the stress, have the tendency to return generally to approximately the original shape.
The blend layer 12 may be any of the blend compositions of the invention. The FIG. 3 structure, as in FIGS. 1 and 2, is designed such that layer 12 may be used as a heat seal layer. A minimum thickness for achieving strong heat seals is likewise about 1 mil in this structure; so that is a preferred minimum thickness. Thicker heat seal layers may advantageously provide more efficient use of the heat seal material, up to about 4 mils; so that is a generally preferred maximum thickness. Layer 12 may also be thicker, as described for the corresponding layer 12 in FIG. 2.
Layer 12 may also be less than 1 mil thick, as, for example, in all the illustrated embodiments, where heat seals are not used or seal strength is not critical.
Turning now to FIG. 4, layer 14 is an abuse resistant layer as in FIG. 2. Layer 12 is of a blend composition of the invention as in FIGS. 1-3. Layer 24 is an oxygen barrier layer such as vinylidene chloride copolymer. Preferred copolymers are vinylidene chloride-vinyl chloride copolymer and vinylidene chloride-methylacrylate copolymer. In the FIG. 4 structure, layer 24 is usually of a thickness of 0.3 to 2.0 mil, depending primarily on the rate of oxygen transmission which is desired for any given end use. While adhesion may be achieved by other means, suitable adhesives, such as the polyester urethane curing adhesives, are usually economically used between the respective layers 12, 24, and 14 to achieve good adhesion between the layers.
For constructing the sheet structure of FIG. 4, layers 12, 24, and 14 are usually formed separately from each other and then combined into the multiple layer structure shown, by conventional techniques for combining polymer films. In a typical process, the layers are joined by conventional adhesive lamination techniques.
As is now evident from the plurality of the multiple layer structures illustrated above, the blend composition of polypropylene and the second and third components has useful advantage in a variety of multiple layer structures. Indeed a layer of the blend composition may advantageously be used in combination with any other layer which may be adhered to it. Thus the multiple layer embodiment of the invention may be generically defined as a multiple layer sheet material wherein the composition of at least one layer is comprised of a blend of polypropylene and the second and third components; and wherein the composition of the other layer or layers need not necessarily be restricted except for purposes of obtaining interlayer adhesion acceptable to the intended use. Thus non-polymeric materials, such as paper and metal foil, and the like, may be used, as well as polymeric materials.
The multiple layer sheet structures of the invention are advantageously formed into packages using heat seals, as illustrated in FIG. 5. Typically, portions of the sheet material are brought into face-to-face relationship, with the layers 12 on each portion facing the opposing sheet portion. Heat seals 28 are then formed between the sheet portions about a common periphery to form a container 30 that generally defines an enclosed area. Usually, one side of the thus formed package is left open, as shown, for insertion of the product. Finally, the filled package is closed and sealed by a heat seal along the open side.
Alternately, the sheet may be formed into a tube by forming a longitudinal seal along overlapping edges; and a transverse seal is also formed across the width of the tube; all as described, for example, in U.S. Pat. No. 4,521,437, herein incorporated by reference. This process is particularly suitable for use in vertical form, fill and seal machines.
In overcoming the primary problem of brittleness of the polypropylene in flexible packages, as addressed herein, a number of actors work together in combination. Important to achievement of the objectives of the invention is incorporation, into the blend composition, of the second component and third components as hereinbefore described. The combined contribution of the second and third components is evidenced by substantially fewer structural failures in the films, sheet structures, and packages made therefrom apparently a result of the second and third components providing, to the blend composition, properties characteristic of elastomers.
The ethylene-based copolymer of the second component is essentially a copolymer of two moieties, both moieties being present in the main chain of the polymer. The overall mole ratio is about 10 to about 95 mole percent ethylene, and conversely about 90 to about 5 mole percent of the second moiety. The ethylene is preferably copolymerized with propylene or butene-1. In the case of propylene, the mole ratio is most preferably within the range of about 20% to about 40% propylene and about 80% to about 60% ethylene. One such material is sold by Mitsui Petrochemical Industries, Ltd. as TAFMER P. In the case of butene-1, the mole ratio is most preferably within the range of about 85% to about 95% ethylene, and about 15% to about 5% butene-1. One such material is sold by Mitsui Petrochemical Industries, Ltd. as TAFMER A. TAFMER P is elastomeric. Tafmer A provides some properties representative of elastomers, as seen in the following EXAMPLES herein.
The third component may be any of the known and readily available elastomeric polymers, or an EBC, indeed even blends thereof. Examples of readily available elastomeric polymers are polybutylene, polyisobutylene, ethylene propylene diene monomr terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, polybutene-1, and isobutylene isoprene copolymer.
The third component is not, however, the same as the second component, as such would effectively make a two-component blend, rather than a three component blend as defined in the invention.
The polypropylene which is used as the first component of the blend provides strength to the sheet structure as well as the capability to withstand high temperature without excessive softening. The inclusion of the second and third components in the blend composition provides resilience to the blend composition.
Any of the polypropylenes may be used in the first component of the blend. Polypropylenes which are copolymers having about 2 to about 8 mole percent ethylene are preferred, as the copolymer provides some minimum level of additional resilience to the polypropylene, as compared to a homopolymer. The term "polypropylene" as used herein is intended to include homopolymers and copolymers except where specified otherwise. Whether the polypropylene is a homopolymer or copolymer, its resilience as demonstrated herein, whether having been retort processed, or not retort processed, is enhanced substantially by the incorporation of the second and third components. Without the incorporation of the second and third components, the polypropylene is at least somewhat rigid, whether homopolymer or copolymer.
For example, a blend of 60% by weight of the polypropylene and 40% polyisobutylene is superior to the same polypropylene when tested in unblended composition, as measured in free fall drop tests of the packages. But these packages with polyisobutylene will fail, at a 9 foot drop with the failure being by rupture through the package wall adjacent a heat seal.
By comparison, packages were made using single-layer film whose composition was 60% by weight of the same polypropylene copolymer, 20% TAFMER A and 20% polyisobutylene, for the same total weight of 40% by weight elastomer as in the above packages using two-component blends. The resulting packages passed the 9 foot drop tests, which passage was not found for either of the 2-component blends.
While polypropylene homopolymer is fully satisfactory for many uses, the polypropylene copolymer is preferred, as it evidences the optimum properties of improved resistance to shock abuse in combination with the capability to withstand elevated processing temperatures. Optimum performance is generally seen, then, in blends of polypropylene copolymer with the second and third components.
While the polypropylene may be present in an amount of about 10% to about 95% by weight, a generally preferred range is about 40% to about 70%. A lower level of about 40% is generally preferred in order to maintain at least a minimal degree of the high heat temperature tolerance of the composition, and a significant moisture vapor barrier, which are provided by polypropylene. An upper level of 70% is generally desired.
While the incorporation of virtually any amount of the second component into the blend composition will provide some benefit, generally, improvement are first evident at a level of about 2% by weight. And while up to about 70% of the second component may be used, the most desired balance of properties is achieved when the second component is present in an amount of about 5% to about 35%.
Likewise, while the incorporation of virtually any amount of the third component into the blend composition will provide some benefit, generally, inprovements are first evident at a level of about 2% by weight. And while up to about 60% of the third component may be used, the most desired balance of properties is achieved when the third component is present in an amount of about 10% to about 40%.
The inter-relationship among the three components is a mystery, in that the use of the second and third components as defined herein may provide a blend having superior properties as compared to the prior art. For whatever unexplained reason, the most preferred family of compositions of the invention is that where each of the components is within its preferred range of compositions; namely about 40% to about 70%. polypropylene, about 5% to about 35% of the second component, and about 10% to about 40% of the third component.
Thus it is seen that the invention provides novel material blend compositions. The invention further provides single layer films and multiple layer films and sheet structures for use in making packages. Indeed, the invention provides heat sealed packages capable of withstanding substantial amounts of physical shock type abuse, which capability is especially noticeable after the closed and sealed packages have been subjected to elevated temperatures of up to about 250° F.

Claims (12)

Having thus described the invention, what is claimed is:
1. A multiple layer sheet structure, comprising:
(a) a first layer, the composition of said first layer having (i) about 40% to about 70% of a first component comprising a polypropylene polymer and having (ii) about 60% to about 30% combined of a second component of a polymeric composition providing elastomeric properties, said polymeric composition comprising a first compositional element chosen from the group consisting of ethylene butene-1 copolymer and ethylene propylene copolymer, and a second compositional element, the composition of said second compositional element being a polymeric modifier providing elastomeric properties; and
(b) a second layer adhered to said first layer, the composition of said second layer being selected from the group consisting of polymers, paper, and metal foil.
2. A multiple layer sheet structure as in claim 1 wherein said first compositional element comprises about 60% to about 95% ethylene.
3. A multiple layer sheet structure as in claim 1 wherein said first compositional element comprises about 60% to about 80% ethylene.
4. A multiple layer sheet structure as in claim 1 wherein said first compositional element comprises about 85% to about 95% ethylene.
5. A multiple layer sheet structure as in any one of claims 1 or 2-4 wherein the composition of said second compositional element is selected from the group consisting of ethylene butene-1 copolymer, ethylene propylene copolymer, polybutylene, polyisobutylene, ethylene propylene diene monomer terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, polybutene-1, and isobutylene isoprene copolymer.
6. A multiple layer sheet structure, comprising:
(a) a first layer, the composition of said first layer having (i) a first component comprising a polypropylene polymer, (ii) as a second component, a polymeric composition providing elastomeric properties, said second component comprising about 60% to about 95% ethylene and conversely about 40% to about 5% of a second moiety chosen from the group consisting of propylene and butene-1, and (iii) a third component, the composition of said third component being a modifier providing elastomeric properties; and
(b) a second layer adhered to said first layer, the composition of said second layer being selected from the group consisting of polymers, paper, and metal foil.
7. A multiple layer sheet structure as in claim 6 wherein said second component comprises about 60% to about 80% ethylene.
8. A multiple layer sheet structure as in claim 6 wherein said second component comprises about 85% to about 95% ethylene.
9. A multiple layer sheet structure as in any one of claims 6-8 wherein the composition of said third component is selected from the group consisting of ethylene butene-1 copolymer, ethylene propylene copolymer, polybutylene polyisobutylene, ethylene propylene diene monomer terpolymer, styrene butadiene styrene copolymer, styrene ethylene butylene styrene copolymer, styrene isoprene styrene copolymer, polybutylene-1, and isobutylene isoprene copolymer.
10. A package made with a sheet structure of any one of claims 1, 2, 4, or 6-8.
11. A package made with a sheet structure of claim 5.
12. A package made with a sheet structure of claim 9.
US07/192,415 1985-11-29 1988-05-05 Multiple layer sheet structures and package Expired - Lifetime US4966795A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US07/192,415 US4966795A (en) 1985-11-29 1988-05-05 Multiple layer sheet structures and package

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/802,910 US4764404A (en) 1985-11-29 1985-11-29 Films having a polypropylene blend layer
US07/192,415 US4966795A (en) 1985-11-29 1988-05-05 Multiple layer sheet structures and package

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US06/802,910 Continuation US4764404A (en) 1985-11-29 1985-11-29 Films having a polypropylene blend layer

Publications (1)

Publication Number Publication Date
US4966795A true US4966795A (en) 1990-10-30

Family

ID=26888058

Family Applications (1)

Application Number Title Priority Date Filing Date
US07/192,415 Expired - Lifetime US4966795A (en) 1985-11-29 1988-05-05 Multiple layer sheet structures and package

Country Status (1)

Country Link
US (1) US4966795A (en)

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5003002A (en) * 1989-08-14 1991-03-26 Rampart Packaging Inc. Blends of amorphous nylon and ethylene vinyl alcohol copolymers and laminates and containers made therefrom
WO1994023941A1 (en) * 1993-04-21 1994-10-27 Mobil Oil Corporation Multilayer packaging films
US5407751A (en) * 1985-11-29 1995-04-18 American National Can Company Easy peel film structure especially for retortable lidstock
EP0738589A2 (en) * 1995-03-22 1996-10-23 W.R. Grace & Co.-Conn. Films for medical solution pouches
US5686527A (en) * 1993-11-16 1997-11-11 Baxter International Inc. Polymeric compositions for medical packaging and devices
US5888648A (en) * 1996-09-12 1999-03-30 Mobil Oil Corporation Multi-layer hermetically sealable film and method of making same
US5935847A (en) 1994-10-28 1999-08-10 Baxter International Inc. Multilayer gas-permeable container for the culture of adherent and non-adherent cells
US5976300A (en) * 1996-07-03 1999-11-02 Baxter International Inc. Method of sealing a port tube in a container
US5998019A (en) * 1993-11-16 1999-12-07 Baxter International Inc. Multi-layered polymer structure for medical products
US6024220A (en) 1995-06-07 2000-02-15 Baxter International Inc. Encapsulated seam for multilayer materials
US6027776A (en) * 1995-03-22 2000-02-22 Cryovac, Inc. Multilayer films for packaging and administering medical solutions
US6068933A (en) * 1996-02-15 2000-05-30 American National Can Company Thermoformable multilayer polymeric film
US6183460B1 (en) 1998-01-22 2001-02-06 Baxter International Inc. Multi-use solution container having flaps
US6297046B1 (en) 1994-10-28 2001-10-02 Baxter International Inc. Multilayer gas-permeable container for the culture of adherent and non-adherent cells
US6319243B1 (en) 1996-09-11 2001-11-20 Baxter International, Inc. Containers and methods for storing and admixing medical solutions
US6372848B1 (en) 2000-10-10 2002-04-16 Baxter International Inc. Blend of ethylene and α-olefin copolymers obtained using a metallocene catalyst for fabricating medical films and tubings
US6391404B1 (en) 1995-06-07 2002-05-21 Baxter International Inc. Coextruded multilayer film materials and containers made therefrom
US6461696B1 (en) 1993-11-16 2002-10-08 Baxter International Inc. Multi-layered polymer based moisture barrier structure for medical grade products
US6528173B1 (en) 1997-02-24 2003-03-04 Baxter International Inc. Coextruded multilayer films for sterilizable fluid containers
US20030064181A1 (en) * 2001-09-07 2003-04-03 Brian Ingraham Peelable film and packaging made therefrom
WO2003080333A1 (en) 2002-03-21 2003-10-02 Baxter International Inc. Multilayered polymer based thin film structure for medical grade products
US6723399B2 (en) 2002-06-12 2004-04-20 Ferro Corporation Medical multilayer film structure
US6743523B1 (en) 2000-03-16 2004-06-01 Baxter International Inc. Multiple layer film of a new non-PVC material
US6835462B2 (en) 2000-03-20 2004-12-28 Avery Dennison Corporation Conformable and die-cuttable biaxially oriented films and labelstocks
US7550185B2 (en) 2001-01-08 2009-06-23 Baxter International Inc. Port tube and closure composition, structure and assembly for a flowable material container
US7731689B2 (en) 2007-02-15 2010-06-08 Baxter International Inc. Dialysis system having inductive heating
US7744554B2 (en) 2002-12-31 2010-06-29 Baxter International Inc. Cassette alignment and integrity testing for dialysis systems
US20100256590A1 (en) * 2009-04-07 2010-10-07 Cryovac, Inc. Multilayer Film for Medical Solution Pouches Having Reduced Proficiency for Forming Bubbles
US7998115B2 (en) 2007-02-15 2011-08-16 Baxter International Inc. Dialysis system having optical flowrate detection
US8105686B2 (en) 2006-07-17 2012-01-31 Avery Dennison Corporation Asymmetric multilayered polymeric film and label stock and label thereof
US8323231B2 (en) 2000-02-10 2012-12-04 Baxter International, Inc. Method and apparatus for monitoring and controlling peritoneal dialysis therapy
US8361023B2 (en) 2007-02-15 2013-01-29 Baxter International Inc. Dialysis system with efficient battery back-up
US8545435B2 (en) 2002-01-03 2013-10-01 Baxter International, Inc. Method and apparatus for providing medical treatment therapy based on calculated demand
US8558964B2 (en) 2007-02-15 2013-10-15 Baxter International Inc. Dialysis system having display with electromagnetic compliance (“EMC”) seal
US8870812B2 (en) 2007-02-15 2014-10-28 Baxter International Inc. Dialysis system having video display with ambient light adjustment
US9636895B2 (en) 2006-06-20 2017-05-02 Avery Dennison Corporation Multilayered polymeric film for hot melt adhesive labeling and label stock and label thereof
US9662867B2 (en) 2006-06-14 2017-05-30 Avery Dennison Corporation Conformable and die-cuttable machine direction oriented labelstocks and labels, and process for preparing
US9676532B2 (en) 2012-08-15 2017-06-13 Avery Dennison Corporation Packaging reclosure label for high alcohol content products
USRE46911E1 (en) 2002-06-26 2018-06-26 Avery Dennison Corporation Machine direction oriented polymeric films and methods of making the same
US11179516B2 (en) 2017-06-22 2021-11-23 Baxter International Inc. Systems and methods for incorporating patient pressure into medical fluid delivery
US11459488B2 (en) 2014-06-02 2022-10-04 Avery Dennison Corporation Films with enhanced scuff resistance, clarity, and conformability

Citations (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2877206A (en) * 1955-12-16 1959-03-10 Phillips Petroleum Co Process for the peroxide treatment of blends of polymers of 1-olefins and hydrogenated diene polymers and products thereof
US3192288A (en) * 1961-08-21 1965-06-29 Exxon Research Engineering Co High impact strength blend of isotactic polypropylene, polyethylene and polyisobutylene
US3299174A (en) * 1963-04-25 1967-01-17 Shell Oil Co Compositions comprising mono-olefin polymers and hydrogenated block copolymers
US3424649A (en) * 1965-09-24 1969-01-28 Shell Oil Co Diene-monovinylarene block copolymerpolyolefin laminates
GB1168541A (en) * 1966-01-28 1969-10-29 Continental Can Co Flexible Packages Containing Non-Fusible High Peel Strength Heat-Seals
US3572721A (en) * 1966-07-22 1971-03-30 Dunlop Co Ltd Play balls
US3665059A (en) * 1967-09-25 1972-05-23 Hercules Inc Polyphase propylene polymer-rubber compositions and process for their preparation
US3689595A (en) * 1970-04-28 1972-09-05 Phillips Petroleum Co High impact polypropylenes
US3701702A (en) * 1970-08-25 1972-10-31 Uniroyal Inc Method of free curing rubber
US3758643A (en) * 1971-01-20 1973-09-11 Uniroyal Inc D polyolefin plastic thermoplastic blend of partially cured monoolefin copolymer rubber an
US3793283A (en) * 1972-03-16 1974-02-19 Shell Oil Co Impact-improved polypropylene compositions
US3806558A (en) * 1971-08-12 1974-04-23 Uniroyal Inc Dynamically partially cured thermoplastic blend of monoolefin copolymer rubber and polyolefin plastic
US3850474A (en) * 1972-03-10 1974-11-26 R Welch Automotive body components
US3862106A (en) * 1971-01-20 1975-01-21 Uniroyal Inc Thermoplastic blend of partially cured monoolefin copolymer rubber and polyolefin plastic
USRE28688E (en) * 1960-10-31 1976-01-20 Raychem Corporation Solid heat-flowable dispersed phase in a crosslinked elastomer
US3937758A (en) * 1973-03-26 1976-02-10 Dart Industries Inc. Process for the production of high impact compositions of polyethylene and polypropylene block copolymers
US3952073A (en) * 1972-06-09 1976-04-20 Toyo Boseki Kabushiki Kaisha Film having good tear property on impact comprising polypropylene and an ethylene polymer
US3962018A (en) * 1973-02-14 1976-06-08 Exxon Research And Engineering Company Polyolefin-elastomer compositions
JPS5272744A (en) * 1975-12-16 1977-06-17 Mitsui Petrochem Ind Ltd Polyprooylene composition wityh good transparency and impact resistanc e
US4104210A (en) * 1975-12-17 1978-08-01 Monsanto Company Thermoplastic compositions of high unsaturation diene rubber and polyolefin resin
US4140162A (en) * 1977-07-28 1979-02-20 Baxter Travenol Lab Clear, autoclavable plastic formulation free of liquid plasticizers
US4147827A (en) * 1977-11-04 1979-04-03 Mobil Oil Corporation Coextruded heat sealable laminar thermoplastic films
JPS54103478A (en) * 1978-02-01 1979-08-14 Tousero Kagaku Kk Thermoplastic film and packaged food therewith
FR2415056A1 (en) * 1978-01-18 1979-08-17 Union Carbide Corp HEAT SHRINK MULTI-LAYER FILM AND PACKAGING BAGS
US4169910A (en) * 1978-06-28 1979-10-02 Union Carbide Corporation Multilayer film including polyolefin layers and a polybutylene layer useful for the production of bags
US4189519A (en) * 1978-08-30 1980-02-19 American Can Company Heat sealable resin blends
US4194039A (en) * 1978-04-17 1980-03-18 W. R. Grace & Co. Multi-layer polyolefin shrink film
US4210686A (en) * 1978-06-19 1980-07-01 Baxter Travenol Laboratories Inc. Multi-layered plastic sheeting having high clarity, strength, and resistance to water vapor transmission
US4230767A (en) * 1978-02-08 1980-10-28 Toyo Boseki Kabushiki Kaisha Heat sealable laminated propylene polymer packaging material
US4250273A (en) * 1977-06-13 1981-02-10 The Firestone Tire & Rubber Company Thermoplastic elastomer blends
GB2055688A (en) * 1979-07-13 1981-03-11 Toyo Boseki Packaging product and the production thereof
US4275120A (en) * 1979-10-05 1981-06-23 Mobil Oil Corporation Heat sealable packaging film comprising propylene polymer substrate and olefin surface layer blend of polybutene-1 and an ethylene or a propylene copolymer
US4291092A (en) * 1979-10-05 1981-09-22 Mobil Oil Corporation Heat sealable packaging film comprising propylene polymer substrate and a surface layer blend of ethylene copolymer and propylene copolymer
US4294889A (en) * 1979-03-28 1981-10-13 Mitsubishi Petrochemical Co., Ltd. Resin compositions and heat-sealable composite biaxially-stretched films
US4311807A (en) * 1980-07-22 1982-01-19 Shell Oil Company Polybutylene modified masterbatches for impact resistant polypropylene
US4322465A (en) * 1980-08-08 1982-03-30 Baxter Travenol Laboratories, Inc. Clear, autoclavable, sealed container having good water vapor barrier properties and flex crack resistance
EP0052557A2 (en) * 1980-11-13 1982-05-26 BP Chimie Société Anonyme Polypropylene compositions with improved impact resistance
US4336212A (en) * 1977-10-11 1982-06-22 Asahi-Dow Limited Composition for drawn film, cold drawn film made of said composition and process for manufacture of said film
US4350795A (en) * 1977-06-13 1982-09-21 The Firestone Tire & Rubber Company Thermoplastic elastomer blends
US4352849A (en) * 1981-03-26 1982-10-05 W. R. Grace & Co. Coextruded, heat-shrinkable, multi-layer, polyolefin packaging film
US4357376A (en) * 1981-07-06 1982-11-02 Union Carbide Corporation Multilayer film for primal meat packaging
JPS58101135A (en) * 1981-12-10 1983-06-16 Idemitsu Petrochem Co Ltd Polypropylene composition
US4389438A (en) * 1980-07-22 1983-06-21 Toyo Ink Manufacturing Co., Ltd. Process for preparing laminates
US4391862A (en) * 1981-07-02 1983-07-05 W. R. Grace & Co., Cryovac Division Pasteurizable thermoplastic film and receptacle therefrom
US4405667A (en) * 1982-08-06 1983-09-20 American Can Company Retortable packaging structure
JPS58157839A (en) * 1982-03-16 1983-09-20 Nippon Oil Co Ltd Impact-resistant polyolefin resin composition
US4407877A (en) * 1974-07-05 1983-10-04 Rasmussen O B High-strength laminate
EP0092897A2 (en) * 1982-04-26 1983-11-02 American National Can Company Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom
US4440815A (en) * 1981-06-29 1984-04-03 Abbott Laboratories Clear, autoclavable plastic formulation for medical liquid containers
US4448792A (en) * 1982-07-26 1984-05-15 W. R. Grace & Co., Cryovac Division Pasteurizable and cook-in shrink bag constructed of a multilayer film
EP0144642A2 (en) * 1983-10-18 1985-06-19 Idemitsu Petrochemical Co. Ltd. A multi-layer film or sheet material
US4528220A (en) * 1984-02-09 1985-07-09 Shell Oil Company Plastic bags for medical solutions and blood
EP0165791A2 (en) * 1984-06-15 1985-12-27 Exxon Research And Engineering Company Composite films and their preparation
US4568723A (en) * 1984-11-08 1986-02-04 Mobil Oil Company Blends of polypropylene, polycarbonate and a saturated styrene-ethylene-butylene-styrene rubber
US4610914A (en) * 1981-08-05 1986-09-09 American Can Company Oriented films of blends of EVOH copolymer
US4621119A (en) * 1984-12-27 1986-11-04 Mobil Oil Corporation Polypropylene-polyethylene-(ethylene-propylene rubber) compositions and films thereof with improved tear strength
US4634735A (en) * 1980-11-13 1987-01-06 Bp Chemicals Limited Polypropylene compositions with high impact strength
US4643926A (en) * 1985-04-29 1987-02-17 W. R. Grace & Co., Cryovac Div. Flexible medical solution pouches
US4769261A (en) * 1987-01-08 1988-09-06 Exxon Chemical Patents Inc. Retort pouch and coextruded film therefor

Patent Citations (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2877206A (en) * 1955-12-16 1959-03-10 Phillips Petroleum Co Process for the peroxide treatment of blends of polymers of 1-olefins and hydrogenated diene polymers and products thereof
USRE28688E (en) * 1960-10-31 1976-01-20 Raychem Corporation Solid heat-flowable dispersed phase in a crosslinked elastomer
US3192288A (en) * 1961-08-21 1965-06-29 Exxon Research Engineering Co High impact strength blend of isotactic polypropylene, polyethylene and polyisobutylene
US3299174A (en) * 1963-04-25 1967-01-17 Shell Oil Co Compositions comprising mono-olefin polymers and hydrogenated block copolymers
US3424649A (en) * 1965-09-24 1969-01-28 Shell Oil Co Diene-monovinylarene block copolymerpolyolefin laminates
GB1168541A (en) * 1966-01-28 1969-10-29 Continental Can Co Flexible Packages Containing Non-Fusible High Peel Strength Heat-Seals
US3572721A (en) * 1966-07-22 1971-03-30 Dunlop Co Ltd Play balls
US3665059A (en) * 1967-09-25 1972-05-23 Hercules Inc Polyphase propylene polymer-rubber compositions and process for their preparation
US3689595A (en) * 1970-04-28 1972-09-05 Phillips Petroleum Co High impact polypropylenes
US3701702A (en) * 1970-08-25 1972-10-31 Uniroyal Inc Method of free curing rubber
US3758643A (en) * 1971-01-20 1973-09-11 Uniroyal Inc D polyolefin plastic thermoplastic blend of partially cured monoolefin copolymer rubber an
US3862106A (en) * 1971-01-20 1975-01-21 Uniroyal Inc Thermoplastic blend of partially cured monoolefin copolymer rubber and polyolefin plastic
US3806558A (en) * 1971-08-12 1974-04-23 Uniroyal Inc Dynamically partially cured thermoplastic blend of monoolefin copolymer rubber and polyolefin plastic
US3850474A (en) * 1972-03-10 1974-11-26 R Welch Automotive body components
US3793283A (en) * 1972-03-16 1974-02-19 Shell Oil Co Impact-improved polypropylene compositions
US3952073A (en) * 1972-06-09 1976-04-20 Toyo Boseki Kabushiki Kaisha Film having good tear property on impact comprising polypropylene and an ethylene polymer
US3962018A (en) * 1973-02-14 1976-06-08 Exxon Research And Engineering Company Polyolefin-elastomer compositions
US3937758A (en) * 1973-03-26 1976-02-10 Dart Industries Inc. Process for the production of high impact compositions of polyethylene and polypropylene block copolymers
US4407877A (en) * 1974-07-05 1983-10-04 Rasmussen O B High-strength laminate
JPS5272744A (en) * 1975-12-16 1977-06-17 Mitsui Petrochem Ind Ltd Polyprooylene composition wityh good transparency and impact resistanc e
US4104210A (en) * 1975-12-17 1978-08-01 Monsanto Company Thermoplastic compositions of high unsaturation diene rubber and polyolefin resin
US4350795A (en) * 1977-06-13 1982-09-21 The Firestone Tire & Rubber Company Thermoplastic elastomer blends
US4250273A (en) * 1977-06-13 1981-02-10 The Firestone Tire & Rubber Company Thermoplastic elastomer blends
US4140162A (en) * 1977-07-28 1979-02-20 Baxter Travenol Lab Clear, autoclavable plastic formulation free of liquid plasticizers
US4336212A (en) * 1977-10-11 1982-06-22 Asahi-Dow Limited Composition for drawn film, cold drawn film made of said composition and process for manufacture of said film
US4147827A (en) * 1977-11-04 1979-04-03 Mobil Oil Corporation Coextruded heat sealable laminar thermoplastic films
FR2415056A1 (en) * 1978-01-18 1979-08-17 Union Carbide Corp HEAT SHRINK MULTI-LAYER FILM AND PACKAGING BAGS
US4196240A (en) * 1978-01-18 1980-04-01 Union Carbide Corporation Heat shrinkable multilayer packaging film of blended copolymers and elastomers
JPS54103478A (en) * 1978-02-01 1979-08-14 Tousero Kagaku Kk Thermoplastic film and packaged food therewith
US4230767A (en) * 1978-02-08 1980-10-28 Toyo Boseki Kabushiki Kaisha Heat sealable laminated propylene polymer packaging material
US4194039A (en) * 1978-04-17 1980-03-18 W. R. Grace & Co. Multi-layer polyolefin shrink film
US4210686A (en) * 1978-06-19 1980-07-01 Baxter Travenol Laboratories Inc. Multi-layered plastic sheeting having high clarity, strength, and resistance to water vapor transmission
US4169910A (en) * 1978-06-28 1979-10-02 Union Carbide Corporation Multilayer film including polyolefin layers and a polybutylene layer useful for the production of bags
US4189519A (en) * 1978-08-30 1980-02-19 American Can Company Heat sealable resin blends
US4294889A (en) * 1979-03-28 1981-10-13 Mitsubishi Petrochemical Co., Ltd. Resin compositions and heat-sealable composite biaxially-stretched films
GB2055688A (en) * 1979-07-13 1981-03-11 Toyo Boseki Packaging product and the production thereof
US4291092A (en) * 1979-10-05 1981-09-22 Mobil Oil Corporation Heat sealable packaging film comprising propylene polymer substrate and a surface layer blend of ethylene copolymer and propylene copolymer
US4275120A (en) * 1979-10-05 1981-06-23 Mobil Oil Corporation Heat sealable packaging film comprising propylene polymer substrate and olefin surface layer blend of polybutene-1 and an ethylene or a propylene copolymer
US4311807A (en) * 1980-07-22 1982-01-19 Shell Oil Company Polybutylene modified masterbatches for impact resistant polypropylene
US4389438A (en) * 1980-07-22 1983-06-21 Toyo Ink Manufacturing Co., Ltd. Process for preparing laminates
US4322465A (en) * 1980-08-08 1982-03-30 Baxter Travenol Laboratories, Inc. Clear, autoclavable, sealed container having good water vapor barrier properties and flex crack resistance
EP0052557A2 (en) * 1980-11-13 1982-05-26 BP Chimie Société Anonyme Polypropylene compositions with improved impact resistance
US4634735A (en) * 1980-11-13 1987-01-06 Bp Chemicals Limited Polypropylene compositions with high impact strength
US4352849A (en) * 1981-03-26 1982-10-05 W. R. Grace & Co. Coextruded, heat-shrinkable, multi-layer, polyolefin packaging film
US4440815A (en) * 1981-06-29 1984-04-03 Abbott Laboratories Clear, autoclavable plastic formulation for medical liquid containers
US4391862A (en) * 1981-07-02 1983-07-05 W. R. Grace & Co., Cryovac Division Pasteurizable thermoplastic film and receptacle therefrom
US4357376A (en) * 1981-07-06 1982-11-02 Union Carbide Corporation Multilayer film for primal meat packaging
US4610914A (en) * 1981-08-05 1986-09-09 American Can Company Oriented films of blends of EVOH copolymer
JPS58101135A (en) * 1981-12-10 1983-06-16 Idemitsu Petrochem Co Ltd Polypropylene composition
JPS58157839A (en) * 1982-03-16 1983-09-20 Nippon Oil Co Ltd Impact-resistant polyolefin resin composition
EP0092897A2 (en) * 1982-04-26 1983-11-02 American National Can Company Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom
US4457960A (en) * 1982-04-26 1984-07-03 American Can Company Polymeric and film structure for use in shrink bags
US4448792A (en) * 1982-07-26 1984-05-15 W. R. Grace & Co., Cryovac Division Pasteurizable and cook-in shrink bag constructed of a multilayer film
US4405667A (en) * 1982-08-06 1983-09-20 American Can Company Retortable packaging structure
EP0144642A2 (en) * 1983-10-18 1985-06-19 Idemitsu Petrochemical Co. Ltd. A multi-layer film or sheet material
US4528220A (en) * 1984-02-09 1985-07-09 Shell Oil Company Plastic bags for medical solutions and blood
EP0165791A2 (en) * 1984-06-15 1985-12-27 Exxon Research And Engineering Company Composite films and their preparation
US4568723A (en) * 1984-11-08 1986-02-04 Mobil Oil Company Blends of polypropylene, polycarbonate and a saturated styrene-ethylene-butylene-styrene rubber
US4621119A (en) * 1984-12-27 1986-11-04 Mobil Oil Corporation Polypropylene-polyethylene-(ethylene-propylene rubber) compositions and films thereof with improved tear strength
US4643926A (en) * 1985-04-29 1987-02-17 W. R. Grace & Co., Cryovac Div. Flexible medical solution pouches
US4769261A (en) * 1987-01-08 1988-09-06 Exxon Chemical Patents Inc. Retort pouch and coextruded film therefor

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Mitsui Petrochemical Industries re Tafmer. *
Shell Technical Literature re Kraton SEBS Copolymer. *

Cited By (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5407751A (en) * 1985-11-29 1995-04-18 American National Can Company Easy peel film structure especially for retortable lidstock
US5003002A (en) * 1989-08-14 1991-03-26 Rampart Packaging Inc. Blends of amorphous nylon and ethylene vinyl alcohol copolymers and laminates and containers made therefrom
WO1994023941A1 (en) * 1993-04-21 1994-10-27 Mobil Oil Corporation Multilayer packaging films
US6168862B1 (en) 1993-11-16 2001-01-02 Baxter International Inc. Multi-layered polymer based thin film structure for medical grade products
US6461696B1 (en) 1993-11-16 2002-10-08 Baxter International Inc. Multi-layered polymer based moisture barrier structure for medical grade products
US5686527A (en) * 1993-11-16 1997-11-11 Baxter International Inc. Polymeric compositions for medical packaging and devices
US6399704B1 (en) 1993-11-16 2002-06-04 Baxter International Inc. Polymeric compositions for medical packaging and devices
US5849843A (en) * 1993-11-16 1998-12-15 Baxter International Inc. Polymeric compositions for medical packaging and devices
US5854347A (en) * 1993-11-16 1998-12-29 Baxter International Inc. Polymeric compositions for medical packaging and devices
US6261655B1 (en) 1993-11-16 2001-07-17 Baxter International Inc. Multi-layered polymer based thin film structure for medical grade products
US6881790B1 (en) 1993-11-16 2005-04-19 Baxter International, Inc. Polymeric compositions for medical packaging and devices
US5998019A (en) * 1993-11-16 1999-12-07 Baxter International Inc. Multi-layered polymer structure for medical products
US6297046B1 (en) 1994-10-28 2001-10-02 Baxter International Inc. Multilayer gas-permeable container for the culture of adherent and non-adherent cells
US5935847A (en) 1994-10-28 1999-08-10 Baxter International Inc. Multilayer gas-permeable container for the culture of adherent and non-adherent cells
US6027776A (en) * 1995-03-22 2000-02-22 Cryovac, Inc. Multilayer films for packaging and administering medical solutions
US5695840A (en) * 1995-03-22 1997-12-09 W. R. Grace & Co.-Conn. Films for medical solution pouches
EP0738589B1 (en) * 1995-03-22 2002-09-25 Cryovac, Inc. Films for medical solution pouches
EP0738589A2 (en) * 1995-03-22 1996-10-23 W.R. Grace & Co.-Conn. Films for medical solution pouches
US6024220A (en) 1995-06-07 2000-02-15 Baxter International Inc. Encapsulated seam for multilayer materials
US6391404B1 (en) 1995-06-07 2002-05-21 Baxter International Inc. Coextruded multilayer film materials and containers made therefrom
US6068933A (en) * 1996-02-15 2000-05-30 American National Can Company Thermoformable multilayer polymeric film
US6562476B2 (en) 1996-02-15 2003-05-13 Pechiney Emballage Flexible Europe Thermoformable multilayer polymeric film
US5976300A (en) * 1996-07-03 1999-11-02 Baxter International Inc. Method of sealing a port tube in a container
US6319243B1 (en) 1996-09-11 2001-11-20 Baxter International, Inc. Containers and methods for storing and admixing medical solutions
US7169138B2 (en) 1996-09-11 2007-01-30 Baxter International Inc. Containers and methods for storing and admixing medical solutions
US5888648A (en) * 1996-09-12 1999-03-30 Mobil Oil Corporation Multi-layer hermetically sealable film and method of making same
US6528173B1 (en) 1997-02-24 2003-03-04 Baxter International Inc. Coextruded multilayer films for sterilizable fluid containers
US6183460B1 (en) 1998-01-22 2001-02-06 Baxter International Inc. Multi-use solution container having flaps
US9474842B2 (en) 2000-02-10 2016-10-25 Baxter International Inc. Method and apparatus for monitoring and controlling peritoneal dialysis therapy
US8323231B2 (en) 2000-02-10 2012-12-04 Baxter International, Inc. Method and apparatus for monitoring and controlling peritoneal dialysis therapy
US10322224B2 (en) 2000-02-10 2019-06-18 Baxter International Inc. Apparatus and method for monitoring and controlling a peritoneal dialysis therapy
US7267885B1 (en) 2000-03-16 2007-09-11 Baxter International Inc. Containers and peelable seal containers of new non-PVC material
US6743523B1 (en) 2000-03-16 2004-06-01 Baxter International Inc. Multiple layer film of a new non-PVC material
US6969483B1 (en) 2000-03-16 2005-11-29 Baxter International Inc. Autoclavable, non-adherent, heat sealable polymer blends for fabricating monolayer and multiple layered films
US6835462B2 (en) 2000-03-20 2004-12-28 Avery Dennison Corporation Conformable and die-cuttable biaxially oriented films and labelstocks
US6372848B1 (en) 2000-10-10 2002-04-16 Baxter International Inc. Blend of ethylene and α-olefin copolymers obtained using a metallocene catalyst for fabricating medical films and tubings
US7550185B2 (en) 2001-01-08 2009-06-23 Baxter International Inc. Port tube and closure composition, structure and assembly for a flowable material container
US6893672B2 (en) 2001-09-07 2005-05-17 Pechiney Emballage Flexible Europe Peelable film and packaging made therefrom
US20030064181A1 (en) * 2001-09-07 2003-04-03 Brian Ingraham Peelable film and packaging made therefrom
US8545435B2 (en) 2002-01-03 2013-10-01 Baxter International, Inc. Method and apparatus for providing medical treatment therapy based on calculated demand
WO2003080333A1 (en) 2002-03-21 2003-10-02 Baxter International Inc. Multilayered polymer based thin film structure for medical grade products
US6723399B2 (en) 2002-06-12 2004-04-20 Ferro Corporation Medical multilayer film structure
USRE46911E1 (en) 2002-06-26 2018-06-26 Avery Dennison Corporation Machine direction oriented polymeric films and methods of making the same
US7744554B2 (en) 2002-12-31 2010-06-29 Baxter International Inc. Cassette alignment and integrity testing for dialysis systems
US8206338B2 (en) 2002-12-31 2012-06-26 Baxter International Inc. Pumping systems for cassette-based dialysis
US9662867B2 (en) 2006-06-14 2017-05-30 Avery Dennison Corporation Conformable and die-cuttable machine direction oriented labelstocks and labels, and process for preparing
US9636895B2 (en) 2006-06-20 2017-05-02 Avery Dennison Corporation Multilayered polymeric film for hot melt adhesive labeling and label stock and label thereof
US8105686B2 (en) 2006-07-17 2012-01-31 Avery Dennison Corporation Asymmetric multilayered polymeric film and label stock and label thereof
US7998115B2 (en) 2007-02-15 2011-08-16 Baxter International Inc. Dialysis system having optical flowrate detection
US8870812B2 (en) 2007-02-15 2014-10-28 Baxter International Inc. Dialysis system having video display with ambient light adjustment
US8558964B2 (en) 2007-02-15 2013-10-15 Baxter International Inc. Dialysis system having display with electromagnetic compliance (“EMC”) seal
US8361023B2 (en) 2007-02-15 2013-01-29 Baxter International Inc. Dialysis system with efficient battery back-up
US9799274B2 (en) 2007-02-15 2017-10-24 Baxter International Inc. Method of controlling medical fluid therapy machine brightness
US7731689B2 (en) 2007-02-15 2010-06-08 Baxter International Inc. Dialysis system having inductive heating
US9302454B2 (en) 2009-04-07 2016-04-05 Cryovac, Inc. Multilayer film for medical solution pouches having reduced proficiency for forming bubbles
US8808595B2 (en) 2009-04-07 2014-08-19 Cryovac, Inc. Multilayer film for medical solution pouches having reduced proficiency for forming bubbles
US20100256590A1 (en) * 2009-04-07 2010-10-07 Cryovac, Inc. Multilayer Film for Medical Solution Pouches Having Reduced Proficiency for Forming Bubbles
US9676532B2 (en) 2012-08-15 2017-06-13 Avery Dennison Corporation Packaging reclosure label for high alcohol content products
US11459488B2 (en) 2014-06-02 2022-10-04 Avery Dennison Corporation Films with enhanced scuff resistance, clarity, and conformability
US11179516B2 (en) 2017-06-22 2021-11-23 Baxter International Inc. Systems and methods for incorporating patient pressure into medical fluid delivery

Similar Documents

Publication Publication Date Title
US4966795A (en) Multiple layer sheet structures and package
US4764404A (en) Films having a polypropylene blend layer
EP0230114B1 (en) Multiple layer polymeric films, packages and flexible containers made therefrom
US4407873A (en) Retortable packaging structure
CA1268108A (en) Multi-layer polymeric films
US4424256A (en) Retortable foil-based packaging structure
US4405667A (en) Retortable packaging structure
US5093164A (en) Multiple layer packaging sheet material
US4640852A (en) Multiple layer films containing oriented layers of nylon and ethylene vinyl alcohol copolymer
USRE35567E (en) Polymeric and film structure for use in shrink bags
US5110642A (en) Films using blends of polypropylene and polyisobutylene
EP0276908A1 (en) Retort pouch and coextruded film therefor
US4892911A (en) Films using blends of polypropylene and polyisobutylene
US4818592A (en) Multiple layer films containing oriented layers of nylon and ethylene vinyl alcohol copolymer
US4986053A (en) Methods of making improved packages
US5073599A (en) Films using blends of polypropylene and polyisobutylene
EP0321172A2 (en) Methods of making multiple layer sheet material packages
EP0230113A2 (en) Polymeric compositions, films and multiple layer structures incorporating the compositions and packages made therefrom
US5154789A (en) Multiple layer films containing oriented layers of nylon and ethylene vinyl alcohol copolymers
EP0229476A1 (en) Polymeric films and processes for making them, multiple layer polymeric films and packages made from the films
US5165988A (en) Laminates and laminated tubes and packages
US5006384A (en) Films using blends of polypropylene and polyisobutylene
EP0346944A2 (en) Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom
AU605115B2 (en) Films of polypropylene blends and polyethylene blends and articles made therewith
JPH0295849A (en) Laminate for retort package

Legal Events

Date Code Title Description
STCF Information on status: patent grant

Free format text: PATENTED CASE

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

AS Assignment

Owner name: PECHINEY PLASTIC PACKAGINC, INC., ILLINOIS

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AMERICAN NATIONAL CAN COMPANY;REEL/FRAME:012463/0131

Effective date: 20011112

AS Assignment

Owner name: PECHINEY PLASTIC PACKAGING, INC., ILLINOIS

Free format text: DUPLICATE RECORDING;ASSIGNOR:AMERICAN NATIONAL CAN COMPANY;REEL/FRAME:012463/0493

Effective date: 20011112

FPAY Fee payment

Year of fee payment: 12

REMI Maintenance fee reminder mailed
AS Assignment

Owner name: PECHINEY EMBALLAGE FLEXIBLE EUROPE, FRANCE

Free format text: RESUBMISSION OF DOCUMENT ID NO 102198992;ASSIGNOR:PECHINEY PLASTIC PACKAGING, INC.;REEL/FRAME:013467/0484

Effective date: 20020117